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US3488716A - Process for the removal of naphthenic acids from petroleum distillate fractions - Google Patents

Process for the removal of naphthenic acids from petroleum distillate fractions Download PDF

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Publication number
US3488716A
US3488716A US672436A US3488716DA US3488716A US 3488716 A US3488716 A US 3488716A US 672436 A US672436 A US 672436A US 3488716D A US3488716D A US 3488716DA US 3488716 A US3488716 A US 3488716A
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Prior art keywords
naphthenic acids
acids
removal
distillate fractions
naphthenic
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US672436A
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Jackson Eng
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ExxonMobil Technology and Engineering Co
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Exxon Research and Engineering Co
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    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G17/00Refining of hydrocarbon oils in the absence of hydrogen, with acids, acid-forming compounds or acid-containing liquids, e.g. acid sludge
    • C10G17/095Refining of hydrocarbon oils in the absence of hydrogen, with acids, acid-forming compounds or acid-containing liquids, e.g. acid sludge with "solid acids", e.g. phosphoric acid deposited on a carrier
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G19/00Refining hydrocarbon oils in the absence of hydrogen, by alkaline treatment
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G29/00Refining of hydrocarbon oils, in the absence of hydrogen, with other chemicals

Definitions

  • the disclosure relates to a catalytic process for the removal of naphthenic acids from petroleum distillate fractions that consists of contacting said fraction with a solid catalyst salt of a Group VIII metal or combination of metal salts, for example, consisting essentially of a metal salt of cobalt molybdate on alumina wherein said solid catalyst comprises a catalyst bed.
  • the conventional process for removing naphthenic acids from distillates is caustic treating.
  • the treatment has a number of disadvantages.
  • sodium naphthenates produced in caustic treating form oil-caustic emulsions which interfere with the treatment and gels are formed which result in oil loss.
  • Small quantities of sodium naphthenates in the oil product cause haze and emulsification.
  • the used caustic solution presents a disposal problem.
  • the object of this invention is to provide a means of removing naphthenic acids from distillate fractions which is characterized by simplicity and low cost.
  • the process of the invention comprises contacting petroleum distillate fractions containing naphthenic acid with a bed of catalyst at mild conditions and recovering a fraction having a significantly reduced acid content. Additional advantages and details of the invention will be apparent from the following description and examples which disclose certain non-limiting embodiments.
  • the process of the invention is applied to petroleum distillate fractions boiling in the range of 200-1000 F., preferably 300-700.”
  • F. The fractions contain from 0.001 to 5.0 wt. percent naphthenic acids.
  • exemplary naphthenic acid-containing fractions include diesel fuel, domestic heating oil, industrial heating oils, and mixtures thereof.
  • Certain lube oil fractions also contain naphthenic acids and they are also suitable feeds for the process.
  • the fractions are obtained by atmospheric or vacuum distillation or by any other appropriate separation means from acid-containing crude oils like those mentioned previously.
  • a conventional reactor adapted for liquid phase, mixed phase, or vapor phase contacting can be used. Ordinarily liquid phase contacting will be employed and the feed is passed downwardly through the catalyst bed.
  • Suitable catalysts include oxides and sulfides of nickel, tungsten, molybdenum, cobalt and iron and combinations thereof distended upon a suitable support material such as alumina, silica-alumina, bauxite, magnesia, and zirconia.
  • a suitable support material such as alumina, silica-alumina, bauxite, magnesia, and zirconia.
  • the most preferred catalyst is cobalt molybdate on alumina.
  • the treating conditions are relatively mild.
  • the temperature ranges from 200-1000 F., preferably 400-800 F. and pressures in the range of from 1 to 1000 p.s.i.g. are suitable.
  • Feed rates can vary depending on the nature of the feed and the other conditions, but rates of 0.5 to 5 v./v./hr. are generally used.
  • Run A Comparing the feed and product of Run A it is seen that the treat reduced the acid number from 0.49 to 0.03. Run B shows that the process is very effective on higher acid number feeds. In both examples the acid number reduction was about 94%.
  • reaction products are a hydrocarbon and Water. This is significant because there is no oil loss as there is in caustic treating.
  • the process of the invention represents an effective, low cost process for eliminating 70100% of the naphthenic acids from distillates without the penalties of yield loss, emulsion formation, and disposal problems connected with caustic treating.
  • the process has obvious advantages over catalytic hydrotreating.
  • a process for removing naphthenic acids from a petroleum fraction comprising the steps of contacting said fraction with a treating agent consisting essentially of a catalyst comprising a salt of a metal selected from the group consisting of nickel, tungsten, molybdenum, cobalt, iron and combinations thereof distended on a suitable support material and recovering a petroleum fraction of reduced naphthenic acid content.
  • a treating agent consisting essentially of a catalyst comprising a salt of a metal selected from the group consisting of nickel, tungsten, molybdenum, cobalt, iron and combinations thereof distended on a suitable support material and recovering a petroleum fraction of reduced naphthenic acid content.
  • a process for removing acids from a petroleum fraction boiling in the range of 300-700 F. containing 0.001- 5.0 wt. percent of said acids consisting essentially of the steps of passing said fraction over a treating agent consisting essentially of a bed of a catalyst comprising cobalt molybdate on alumina in the liquid phase, at a tempera- References Cited UNITED STATES PATENTS 2/1956 Miller et al 19624 9/1967 Eng et al. 208-238 10 DELBERT E. GANTZ, Primary Examiner S. M. NELSON, Assistant Examiner

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  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
  • Catalysts (AREA)

Description

United States Patent 3,488,716 PROCESS FOR THE REMOVAL OF N APHTHENIC ACIDS FROM PETROLEUM DISTILLATE FRACTIONS Jackson Eng, Sarnia Township, Lambton County, Ontario, Canada, assignor to Esso Research and Engineering Company, a corporation of Delaware No Drawing. Filed Oct. 3, 1967, Ser. No. 672,436 Int. Cl. Cl0g 29/06 US. Cl. 208-263 5 Claims ABSTRACT OF THE DISCLOSURE The disclosure relates to a catalytic process for the removal of naphthenic acids from petroleum distillate fractions that consists of contacting said fraction with a solid catalyst salt of a Group VIII metal or combination of metal salts, for example, consisting essentially of a metal salt of cobalt molybdate on alumina wherein said solid catalyst comprises a catalyst bed.
Some crude oils such as Tia Juana Medium, Colombian De Mares, San Jaoquin Valley and Baku contain napthenic acids. Distillates produced from these crudes must be treated to remove these acids. Otherwise, the acids will corrode the storage tanks, the piping, and the equipment in which the distillate products are used.
The conventional process for removing naphthenic acids from distillates is caustic treating. The treatment has a number of disadvantages. For example, sodium naphthenates produced in caustic treating form oil-caustic emulsions which interfere with the treatment and gels are formed which result in oil loss. Small quantities of sodium naphthenates in the oil product cause haze and emulsification. Furthermore, the used caustic solution presents a disposal problem.
The prior art also discloses that naphthenic acids can be removed from distillates by catalytic hydrotreating. However, the expense of supplying and circulating hydrogen limits the use of this technique.
The object of this invention is to provide a means of removing naphthenic acids from distillate fractions which is characterized by simplicity and low cost.
Briefly summarizing, the process of the invention comprises contacting petroleum distillate fractions containing naphthenic acid with a bed of catalyst at mild conditions and recovering a fraction having a significantly reduced acid content. Additional advantages and details of the invention will be apparent from the following description and examples which disclose certain non-limiting embodiments.
The process of the invention is applied to petroleum distillate fractions boiling in the range of 200-1000 F., preferably 300-700." F. The fractions contain from 0.001 to 5.0 wt. percent naphthenic acids. Exemplary naphthenic acid-containing fractions include diesel fuel, domestic heating oil, industrial heating oils, and mixtures thereof. Certain lube oil fractions also contain naphthenic acids and they are also suitable feeds for the process. The fractions are obtained by atmospheric or vacuum distillation or by any other appropriate separation means from acid-containing crude oils like those mentioned previously.
A conventional reactor adapted for liquid phase, mixed phase, or vapor phase contacting can be used. Ordinarily liquid phase contacting will be employed and the feed is passed downwardly through the catalyst bed.
Suitable catalysts include oxides and sulfides of nickel, tungsten, molybdenum, cobalt and iron and combinations thereof distended upon a suitable support material such as alumina, silica-alumina, bauxite, magnesia, and zirconia. The most preferred catalyst is cobalt molybdate on alumina.
The treating conditions are relatively mild. The temperature ranges from 200-1000 F., preferably 400-800 F. and pressures in the range of from 1 to 1000 p.s.i.g. are suitable. Feed rates can vary depending on the nature of the feed and the other conditions, but rates of 0.5 to 5 v./v./hr. are generally used.
The following examples illustrate the invention.
Two liquid phase runs were made on Tia Juana Medium Gas Oil boiling in the range of 380-600 F. This distillate has an acid number of 0.49 (about 0.22 wt. percent acid). For Run B the gas oil was spiked with naphthenic acid to increase its acid number about tenfold. Treating conditions in the downflow laboratory reactor included a temperature of 650 F., a pressure of 200 p.s.i.g., and a space velocity (LHSV) of 4 v./v./hr. The catalyst was cobalt molybdate on alumina (Nalcomo 471, Nalco, Chicago, 111.).
TABLE I Tia Juana Med. Tia Juana Med. Gas Oil 2 plus Gas Oil Naph. Acids Run Feed Feed Product Feed Product {Mg KOH requiredto neutralize naphthenic acids in 1 gm. of oil (1 ac g )number approxmlately equivalent to 0.45 wt. percent naphthenic am 5 Sufiicient naphthenic acids added to bring Tia Juana Medium gas 011 up to 5 acid number.
Comparing the feed and product of Run A it is seen that the treat reduced the acid number from 0.49 to 0.03. Run B shows that the process is very effective on higher acid number feeds. In both examples the acid number reduction was about 94%.
Without wishing to be bound thereby it is felt that the mechanism of the reaction is as follows:
(C 2)NCO0H U (CH2) CH3 H20 (Typical Naphthenie Acid) Thus the reaction products are a hydrocarbon and Water. This is significant because there is no oil loss as there is in caustic treating.
The process of the invention represents an effective, low cost process for eliminating 70100% of the naphthenic acids from distillates without the penalties of yield loss, emulsion formation, and disposal problems connected with caustic treating. The process has obvious advantages over catalytic hydrotreating.
What is claimed is:
1. A process for removing naphthenic acids from a petroleum fraction comprising the steps of contacting said fraction with a treating agent consisting essentially of a catalyst comprising a salt of a metal selected from the group consisting of nickel, tungsten, molybdenum, cobalt, iron and combinations thereof distended on a suitable support material and recovering a petroleum fraction of reduced naphthenic acid content.
2. Process according to claim 1 in which the fraction is a gas oil containing 0.00 1-5 .0 Wt. percent naphthenic acid.
3. Process according to claim 1 in which said contacting is in the liquid phase.
4. Process according to claim 1 in which the catalyst is cobalt molybdate on alumina.
5. A process for removing acids from a petroleum fraction boiling in the range of 300-700 F. containing 0.001- 5.0 wt. percent of said acids consisting essentially of the steps of passing said fraction over a treating agent consisting essentially of a bed of a catalyst comprising cobalt molybdate on alumina in the liquid phase, at a tempera- References Cited UNITED STATES PATENTS 2/1956 Miller et al 19624 9/1967 Eng et al. 208-238 10 DELBERT E. GANTZ, Primary Examiner S. M. NELSON, Assistant Examiner
US672436A 1967-10-03 1967-10-03 Process for the removal of naphthenic acids from petroleum distillate fractions Expired - Lifetime US3488716A (en)

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Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3996130A (en) * 1974-01-03 1976-12-07 Nikolai Sergeevich Nametkin Method of purifying crude petroleum and primary refining products
WO1996006899A1 (en) * 1994-08-29 1996-03-07 Den Norske Stats Oljeselskap A.S A process for removing essentially naphthenic acids from a hydrocarbon oil
US5871636A (en) * 1997-08-29 1999-02-16 Exxon Research And Engineering Company Catalytic reduction of acidity of crude oils in the absence of hydrogen
US5910242A (en) * 1997-08-29 1999-06-08 Exxon Research And Engineering Company Process for reduction of total acid number in crude oil
WO2003040265A1 (en) * 2001-11-08 2003-05-15 Conocophillips Company Acidic petroleum oil treatment
KR100451614B1 (en) * 1995-10-20 2004-11-20 엑손 리써치 앤드 엔지니어링 컴파니 Pyrolysis method of naphthenic acid
CN117186940A (en) * 2022-05-31 2023-12-08 中国石油化工股份有限公司 A method for reducing the acid value of hydrocarbon raw materials

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5928502A (en) * 1997-08-29 1999-07-27 Exxon Research And Engineering Co. Process for reducing total acid number of crude oil
WO1999010451A1 (en) * 1997-08-29 1999-03-04 Exxon Research And Engineering Company Process for reducing total acid number of crude oil
US7745369B2 (en) 2003-12-19 2010-06-29 Shell Oil Company Method and catalyst for producing a crude product with minimal hydrogen uptake
BRPI0405587A (en) 2003-12-19 2005-10-04 Shell Int Research Methods of Producing a Transportable Fuel and Crude Oil Product, Heating Fuel, Lubricants or Chemicals, and Crude Oil Product
US8241489B2 (en) 2003-12-19 2012-08-14 Shell Oil Company Systems, methods, and catalysts for producing a crude product
CN101624543A (en) * 2003-12-19 2010-01-13 国际壳牌研究有限公司 Crude oil products, and methods of producing transportation fuels, heating fuels, lubricants, or chemicals
US20100098602A1 (en) 2003-12-19 2010-04-22 Opinder Kishan Bhan Systems, methods, and catalysts for producing a crude product
RU2424275C2 (en) 2005-04-11 2011-07-20 Шелл Интернэшнл Рисерч Маатсхаппий Б.В. Procedure for production of semi-finished product with reduced content of micro-carbon residue and catalyst for its implementation
US7678264B2 (en) 2005-04-11 2010-03-16 Shell Oil Company Systems, methods, and catalysts for producing a crude product
US20080083650A1 (en) 2006-10-06 2008-04-10 Bhan Opinder K Methods for producing a crude product

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2734019A (en) * 1956-02-07 Hydrofining naphthenic lubricating oil
US3340184A (en) * 1964-10-30 1967-09-05 Exxon Research Engineering Co Process for removing sulfur from petroleum oils and synthesizing mercaptans

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2734019A (en) * 1956-02-07 Hydrofining naphthenic lubricating oil
US3340184A (en) * 1964-10-30 1967-09-05 Exxon Research Engineering Co Process for removing sulfur from petroleum oils and synthesizing mercaptans

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3996130A (en) * 1974-01-03 1976-12-07 Nikolai Sergeevich Nametkin Method of purifying crude petroleum and primary refining products
WO1996006899A1 (en) * 1994-08-29 1996-03-07 Den Norske Stats Oljeselskap A.S A process for removing essentially naphthenic acids from a hydrocarbon oil
CN1051569C (en) * 1994-08-29 2000-04-19 挪威国家石油公司 Process for removing essentially naphthenic acids from hydrocarbon oil
KR100451614B1 (en) * 1995-10-20 2004-11-20 엑손 리써치 앤드 엔지니어링 컴파니 Pyrolysis method of naphthenic acid
US5871636A (en) * 1997-08-29 1999-02-16 Exxon Research And Engineering Company Catalytic reduction of acidity of crude oils in the absence of hydrogen
US5910242A (en) * 1997-08-29 1999-06-08 Exxon Research And Engineering Company Process for reduction of total acid number in crude oil
WO2003040265A1 (en) * 2001-11-08 2003-05-15 Conocophillips Company Acidic petroleum oil treatment
CN117186940A (en) * 2022-05-31 2023-12-08 中国石油化工股份有限公司 A method for reducing the acid value of hydrocarbon raw materials
CN117186940B (en) * 2022-05-31 2025-10-10 中国石油化工股份有限公司 A method for reducing the acid value of hydrocarbon raw materials

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